Canonical Allele Identifier: CA431391722

Gene: BARD1

Linked Data

• MyVariant Identifiers: chr2:g.215645701A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214780977A>T , CM000664.2:g.214780977A>T	GRCh38
NC_000002.11:g.215645701A>T , CM000664.1:g.215645701A>T	GRCh37
NC_000002.10:g.215353946A>T	NCBI36
NG_012047.2:g.33728T>A
NG_012047.3:g.33735T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260947.9:c.897T>A MANE Select	ENSP00000260947.4:p.Thr299=
ENST00000421162.2:c.215+16084T>A	ENSP00000392245.2:n.215+16084T>A
ENST00000613192.2:c.158+28435T>A	ENSP00000483275.2:n.158+28435T>A
ENST00000613374.5:c.159-28422T>A	ENSP00000484464.1:n.159-28422T>A
ENST00000613706.5:c.897T>A	ENSP00000484976.2:p.Thr299=
ENST00000617164.5:c.840T>A	ENSP00000480470.1:p.Thr280=
ENST00000619009.5:c.364+11320T>A	ENSP00000482293.1:n.364+11320T>A
ENST00000650978.1:c.739T>A
ENST00000260947.8:c.897T>A	ENSP00000260947.4:p.Thr299=
ENST00000421162.1:c.215+16084T>A	ENSP00000392245.1:n.215+16084T>A
ENST00000455743.5:c.*517T>A	ENSP00000412186.1:n.*517T>A
ENST00000471787.1:n.792T>A
ENST00000613192.1:c.73+28435T>A	ENSP00000483275.1:n.73+28435T>A
ENST00000613374.4:c.159-28422T>A	ENSP00000484464.1:n.159-28422T>A
ENST00000613706.4:c.215+16084T>A	ENSP00000484976.1:n.215+16084T>A
ENST00000617164.4:c.840T>A	ENSP00000480470.1:p.Thr280=
ENST00000619009.4:c.364+11320T>A	ENSP00000482293.1:n.364+11320T>A
ENST00000620057.4:c.364+11320T>A	ENSP00000481988.1:n.364+11320T>A
NM_000465.3:c.897T>A	NP_000456.2:p.Thr299=
NM_001282543.1:c.840T>A	NP_001269472.1:p.Thr280=
NM_001282545.1:c.215+16084T>A	NP_001269474.1:n.215+16084T>A
NM_001282548.1:c.159-28422T>A	NP_001269477.1:n.159-28422T>A
NM_001282549.1:c.364+11320T>A	NP_001269478.1:n.364+11320T>A
NR_104212.1:n.890T>A
NR_104215.1:n.833T>A
NR_104216.1:n.506+11320T>A
XM_011511567.1:c.843T>A	XP_011509869.1:p.Thr281=
XM_011511568.1:c.897T>A	XP_011509870.1:p.Thr299=
XM_017004613.1:c.996T>A	XP_016860102.1:p.Thr332=
XM_017004614.1:c.996T>A	XP_016860103.1:p.Thr332=
XR_002959322.1:n.1087T>A
NM_000465.4:c.897T>A MANE Select	NP_000456.2:p.Thr299=
NM_001282543.2:c.840T>A	NP_001269472.1:p.Thr280=
NM_001282545.2:c.215+16084T>A	NP_001269474.1:n.215+16084T>A
NM_001282548.2:c.159-28422T>A	NP_001269477.1:n.159-28422T>A
NM_001282549.2:c.364+11320T>A	NP_001269478.1:n.364+11320T>A
NR_104212.2:n.862T>A
NR_104215.2:n.805T>A
NR_104216.2:n.478+11320T>A